Skip to main content
Top
Published in: Neuroradiology 10/2008

01-10-2008 | Functional Neuroradiology

Spinal fMRI during proprioceptive and tactile tasks in healthy subjects: activity detected using cross-correlation, general linear model and independent component analysis

Authors: P. Valsasina, F. Agosta, D. Caputo, P. W. Stroman, M. Filippi

Published in: Neuroradiology | Issue 10/2008

Login to get access

Abstract

Introduction

Functional MRI (fMRI) of the spinal cord is able to provide maps of neuronal activity. Spinal fMRI data have been analyzed in previous studies by calculating the cross-correlation (CC) between the stimulus and the time course of every voxel and, more recently, by using the general linear model (GLM). The aim of this study was to compare three different approaches (CC analysis, GLM and independent component analysis (ICA)) for analyzing fMRI scans of the cervical spinal cord.

Methods

We analyzed spinal fMRI data from healthy subjects during a proprioceptive and a tactile stimulation by using two model-based approaches, i.e., CC analysis between the stimulus shape and the time course of every voxel, and the GLM. Moreover, we applied independent component analysis, a model-free approach which decomposes the data in a set of source signals.

Results

All methods were able to detect cervical cord areas of activity corresponding to the expected regions of neuronal activations. Model-based approaches (CC and GLM) revealed similar patterns of activity. ICA could identify a component correlated to fMRI stimulation, although with a lower statistical threshold than model-based approaches, and many components, consistent across subjects, which are likely to be secondary to noise present in the data.

Conclusions

Model-based approaches seem to be more robust for estimating task-related activity, whereas ICA seems to be useful for eliminating noise components from the data. Combined use of ICA and GLM might improve the reliability of spinal fMRI results.
Literature
1.
go back to reference Ogawa S, Lee TM, Nayak AS et al (1990) Oxygenation-sensitive contrast in magnetic resonance image of rodent brain at high magnetic fields. Magn Reson Med 14:68–78PubMedCrossRef Ogawa S, Lee TM, Nayak AS et al (1990) Oxygenation-sensitive contrast in magnetic resonance image of rodent brain at high magnetic fields. Magn Reson Med 14:68–78PubMedCrossRef
2.
go back to reference Stroman PW (2005) Magnetic resonance imaging of neuronal function in the spinal cord: spinal fMRI. Clin Med Res 3:146–156PubMedCrossRef Stroman PW (2005) Magnetic resonance imaging of neuronal function in the spinal cord: spinal fMRI. Clin Med Res 3:146–156PubMedCrossRef
3.
go back to reference Stroman PW, Ryner LN (2001) Functional MRI of motor and sensory activation in the human spinal cord. Magn Reson Imaging 19:27–32PubMedCrossRef Stroman PW, Ryner LN (2001) Functional MRI of motor and sensory activation in the human spinal cord. Magn Reson Imaging 19:27–32PubMedCrossRef
4.
go back to reference Komisaruk BR, Mosier KM, Liu WC et al (2002) Functional localization of brainstem and cervical spinal cord nuclei in humans with fMRI. AJNR Am J Neuroradiol 23:609–617PubMed Komisaruk BR, Mosier KM, Liu WC et al (2002) Functional localization of brainstem and cervical spinal cord nuclei in humans with fMRI. AJNR Am J Neuroradiol 23:609–617PubMed
5.
go back to reference Li G, Ng MC, Wong KK et al (2005) Spinal effects of acupuncture stimulation assessed by proton density-weighted functional magnetic resonance imaging at 0.2 T. Magn Reson Imaging 23:995–999PubMedCrossRef Li G, Ng MC, Wong KK et al (2005) Spinal effects of acupuncture stimulation assessed by proton density-weighted functional magnetic resonance imaging at 0.2 T. Magn Reson Imaging 23:995–999PubMedCrossRef
6.
go back to reference Govers N, Beghin J, Van Goethem JW et al (2007) Functional MRI of the cervical spinal cord on 1.5 T with fingertapping: to what extent is it feasible? Neuroradiology 49:73–81PubMedCrossRef Govers N, Beghin J, Van Goethem JW et al (2007) Functional MRI of the cervical spinal cord on 1.5 T with fingertapping: to what extent is it feasible? Neuroradiology 49:73–81PubMedCrossRef
7.
go back to reference Maieron M, Iannetti GD, Bodurka J et al (2007) Functional responses in the human spinal cord during willed motor actions: evidence for side- and rate-dependent activity. J Neurosci 27:4182–4190PubMedCrossRef Maieron M, Iannetti GD, Bodurka J et al (2007) Functional responses in the human spinal cord during willed motor actions: evidence for side- and rate-dependent activity. J Neurosci 27:4182–4190PubMedCrossRef
8.
go back to reference Agosta F, Valsasina P, Caputo D et al (2007) Tactile-associated fMRI recruitment of the cervical cord in healthy subjects. Hum Brain Mapp In press. DOI 10.1002/hbm.20499 Agosta F, Valsasina P, Caputo D et al (2007) Tactile-associated fMRI recruitment of the cervical cord in healthy subjects. Hum Brain Mapp In press. DOI 10.​1002/​hbm.​20499
9.
go back to reference Stroman PW (2006) Discrimination of errors from neuronal activity in functional MRI of the human spinal cord by means of General Linear Model analysis. Magn Reson Med 56:452–456PubMedCrossRef Stroman PW (2006) Discrimination of errors from neuronal activity in functional MRI of the human spinal cord by means of General Linear Model analysis. Magn Reson Med 56:452–456PubMedCrossRef
10.
go back to reference Ng MC, Wong KK, Li G et al (2006) Proton-density-weighted spinal fMRI with sensorimotor stimulation at 0.2 T. NeuroImage 29:995–999PubMedCrossRef Ng MC, Wong KK, Li G et al (2006) Proton-density-weighted spinal fMRI with sensorimotor stimulation at 0.2 T. NeuroImage 29:995–999PubMedCrossRef
11.
go back to reference Kornelsen J, Stroman PW (2004) FMRI of the lumbar spinal cord during a lower limb motor task. Magn Reson Med 52:411–414PubMedCrossRef Kornelsen J, Stroman PW (2004) FMRI of the lumbar spinal cord during a lower limb motor task. Magn Reson Med 52:411–414PubMedCrossRef
12.
go back to reference Lawrence JM, Stroman PW, Kollias SS (2008) Functional magnetic resonance imaging of the human spinal cord during vibration stimulation of different dermatomes. Neuroradiology 50:273–280PubMedCrossRef Lawrence JM, Stroman PW, Kollias SS (2008) Functional magnetic resonance imaging of the human spinal cord during vibration stimulation of different dermatomes. Neuroradiology 50:273–280PubMedCrossRef
13.
go back to reference Bandettini PA, Jesmanowicz A, Wong EC et al (1993) Processing strategies for time-course data sets in functional MRI of the human brain. Magn Reson Med 30:161–173PubMedCrossRef Bandettini PA, Jesmanowicz A, Wong EC et al (1993) Processing strategies for time-course data sets in functional MRI of the human brain. Magn Reson Med 30:161–173PubMedCrossRef
14.
go back to reference Friston KJ, Jezzard P, Turner R (1994) Analysis of functional MRI time series. Hum Brain Mapp 1:153–171CrossRef Friston KJ, Jezzard P, Turner R (1994) Analysis of functional MRI time series. Hum Brain Mapp 1:153–171CrossRef
15.
go back to reference McKeown MJ, Makeig S, Brown GG et al (1998) Analysis of fMRI data by blind separation into independent spatial components. Hum Brain Mapp 6:160–188PubMedCrossRef McKeown MJ, Makeig S, Brown GG et al (1998) Analysis of fMRI data by blind separation into independent spatial components. Hum Brain Mapp 6:160–188PubMedCrossRef
16.
go back to reference Calhoun VD, Adali T, Pearlson GD et al (2001) A method for making group inferences from functional MRI data using independent component analysis. Hum Brain Mapp 14:140–151PubMedCrossRef Calhoun VD, Adali T, Pearlson GD et al (2001) A method for making group inferences from functional MRI data using independent component analysis. Hum Brain Mapp 14:140–151PubMedCrossRef
17.
go back to reference DeLuca M, Beckmann CF, De Stefano N et al (2006) FMRI resting state networks define distinct modes of long-distance interactions in the human brain. NeuroImage 29:1359–1367CrossRef DeLuca M, Beckmann CF, De Stefano N et al (2006) FMRI resting state networks define distinct modes of long-distance interactions in the human brain. NeuroImage 29:1359–1367CrossRef
18.
go back to reference Brooks JC, Beckmann CF, Miller KL et al (2008) Physiological noise modeling for spinal functional magnetic resonance imaging studies. NeuroImage 39:680–692PubMedCrossRef Brooks JC, Beckmann CF, Miller KL et al (2008) Physiological noise modeling for spinal functional magnetic resonance imaging studies. NeuroImage 39:680–692PubMedCrossRef
19.
go back to reference Calhoun VD, Adali T, McGinty B et al (2001) FMRI activation in a visual-perception task: network of areas detected using the General Linear Model and Independent Component Analysis. NeuroImage 14:1080–1088PubMedCrossRef Calhoun VD, Adali T, McGinty B et al (2001) FMRI activation in a visual-perception task: network of areas detected using the General Linear Model and Independent Component Analysis. NeuroImage 14:1080–1088PubMedCrossRef
20.
go back to reference Bell AJ, Sejnowski TJ (1995) An information maximization approach to blind separation and blind deconvolution. Neural Comput 7:1129–1159PubMedCrossRef Bell AJ, Sejnowski TJ (1995) An information maximization approach to blind separation and blind deconvolution. Neural Comput 7:1129–1159PubMedCrossRef
21.
go back to reference Stroman PW, Krause V, Malisza KL et al (2002) Extravascular proton-density changes as non-BOLD component of contrast in fMRI of the human spinal cord. Magn Reson Med 48:122–127PubMedCrossRef Stroman PW, Krause V, Malisza KL et al (2002) Extravascular proton-density changes as non-BOLD component of contrast in fMRI of the human spinal cord. Magn Reson Med 48:122–127PubMedCrossRef
22.
go back to reference Stroman PW, Tomanek B, Krause V et al (2003) Functional magnetic resonance imaging of the human brain based on signal enhancement by extravascular protons (SEEP fMRI). Magn Reson Med 49:433–439PubMedCrossRef Stroman PW, Tomanek B, Krause V et al (2003) Functional magnetic resonance imaging of the human brain based on signal enhancement by extravascular protons (SEEP fMRI). Magn Reson Med 49:433–439PubMedCrossRef
23.
go back to reference Stroman PW, Kornelsen J, Lawrence J et al (2005) Functional magnetic resonance imaging based on SEEP contrast: response function and anatomical specificity. Magn Reson Imaging 23:843–850PubMedCrossRef Stroman PW, Kornelsen J, Lawrence J et al (2005) Functional magnetic resonance imaging based on SEEP contrast: response function and anatomical specificity. Magn Reson Imaging 23:843–850PubMedCrossRef
24.
go back to reference Brodal A (1981) Neurological anatomy in relation to clinical medicine. In: New York: Oxford University Press (eds) Brodal A (1981) Neurological anatomy in relation to clinical medicine. In: New York: Oxford University Press (eds)
25.
go back to reference Kandel E, Schwartz JH, Jessell TM (1991) Principles of neural science. New York: Elsevier Science Publishing Company, Inc (eds) Kandel E, Schwartz JH, Jessell TM (1991) Principles of neural science. New York: Elsevier Science Publishing Company, Inc (eds)
26.
go back to reference Stracke CP, Pettersson LG, Schoth F et al (2005) Interneuronal systems of the cervical spinal cord assessed with BOLD imaging ad 1.5 T. Neuroradiology 47:127–133PubMedCrossRef Stracke CP, Pettersson LG, Schoth F et al (2005) Interneuronal systems of the cervical spinal cord assessed with BOLD imaging ad 1.5 T. Neuroradiology 47:127–133PubMedCrossRef
27.
go back to reference Brooks J, Robson M, Schweinhardt P et al (2004) Functional magnetic resonance imaging (fMRI) of the spinal cord: a methodological study. In: Proceedings of the 23rd annual meeting of the American Pain Society, Vancouver, Canada. (abstract 667) Brooks J, Robson M, Schweinhardt P et al (2004) Functional magnetic resonance imaging (fMRI) of the spinal cord: a methodological study. In: Proceedings of the 23rd annual meeting of the American Pain Society, Vancouver, Canada. (abstract 667)
28.
go back to reference McGonigle D, Howseman A, Athwal B et al (2000) Variability in fMRI: an examination of intersession differences. NeuroImage 11:708–734PubMedCrossRef McGonigle D, Howseman A, Athwal B et al (2000) Variability in fMRI: an examination of intersession differences. NeuroImage 11:708–734PubMedCrossRef
29.
Metadata
Title
Spinal fMRI during proprioceptive and tactile tasks in healthy subjects: activity detected using cross-correlation, general linear model and independent component analysis
Authors
P. Valsasina
F. Agosta
D. Caputo
P. W. Stroman
M. Filippi
Publication date
01-10-2008
Publisher
Springer-Verlag
Published in
Neuroradiology / Issue 10/2008
Print ISSN: 0028-3940
Electronic ISSN: 1432-1920
DOI
https://doi.org/10.1007/s00234-008-0420-8

Other articles of this Issue 10/2008

Neuroradiology 10/2008 Go to the issue

Interventional Neuroradiology

Brain imaging with a flat detector C-arm